HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376631Generated: November 2, 2026
Aminoisobutyric acid → HCID 22916684, compound
https://huagongshe.com/reaction/1376631
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aminoisobutyric acid | HCID 6119 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Thiazol-2-ylmethanamine | HCID 2756507 | — |
| Product | HCID 22916684 | HCID 22916684 | 96.6% |
Reaction Steps
To 2.5 g (0.024m mole) of 2-amino-2-methylpropanoic acid was added under ice-cooling 17 ml (0.122 mole) of triethylamine, followed by 15 ml (0.14 mole) of ethyl trifluoroacetate, and the mixture was stirred for 1 hour. Six milliliter (0.05 mole) of ethyl trifluoroacetate was added, and the mixture was further stirred for 20 hours. The reaction mixture was concentrated to dryness under reduced pressure. To the solution of the residue thus obtained in methylene chloride (20 ml) was added 5 g (0.036 mole) of 1-hydroxybenzotriazole at a temperature of 3° C., followed by 38 ml (0.036 mole) of 1.0M dicyclohexylcarbodiimide and 2.85 g (0.025 mole) of 2-aminomethylthiazole. The mixture was treated in the same manner as in Preparation 16 (a) to give 4.9 g of the title compound. Yield 66%. NMR (CDCl3) δ: 1.71 (6H, s), 4.80 (2H, d, J=5.6 Hz), 7.03 (1H, brs), 7.33 (1H, d, J=3.3 Hz), 7.72 (1H, d, J=3.3 Hz), 7.81 (1H, brs).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663162 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-a851ce9be1a243af88a29265650b898d |
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| Source note | uspto-grants-1997_09 |
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